Publications:

Whole genome sequencing identifies high-impact variants in well-known pharmacogenomic genes.

The Pharmacogenomics Journal

Choi, Jihoon J; Tantisira, Kelan G KG; Duan, Qing Ling QL

Publication Date: 2019-04

Variant appearance in text: rs6685578

PubMed Link: 30214008

Variant Present in the following documents:

• NIHMS1503453-supplement-3.xlsx, sheet 1

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Targeted next-generation resequencing of f5 gene identifies novel multiple variants pattern in severe hereditary factor v deficiency.

Case Reports In Genetics

Janicki, Piotr K PK; Vaida, Sonia S; Al-Mondhiry, Hamid A B HA

Publication Date: 2013

Variant appearance in text: rs6685578

PubMed Link: 23662219

Variant Present in the following documents:

• Main text
• CRIM.GENETICS2013-941684.pdf

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